Canonical Allele Identifier: CA168086668

Gene: BRAF

Linked Data

• dbSNP Id: rs529437865
• MyVariant Identifiers: chr7:g.140477096_140477097del (hg19) ; chr7:g.140777296_140777297del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777297_140777298del , CM000669.2:g.140777297_140777298del	GRCh38
NC_000007.13:g.140477097_140477098del , CM000669.1:g.140477097_140477098del	GRCh37
NC_000007.12:g.140123566_140123567del	NCBI36
NG_007873.3:g.152468_152469del , LRG_299:g.152468_152469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1518-209_1518-208del MANE Select	ENSP00000493543.1:n.1518-209_1518-208del
ENST00000288602.11:c.1638-209_1638-208del	ENSP00000288602.7:n.1638-209_1638-208del
ENST00000479537.6:c.188-209_188-208del
ENST00000496384.7:c.1518-209_1518-208del	ENSP00000419060.2:n.1518-209_1518-208del
ENST00000497784.2:c.*968-209_*968-208del	ENSP00000420119.2:n.*968-209_*968-208del
ENST00000642228.1:c.*596-209_*596-208del	ENSP00000493678.1:n.*596-209_*596-208del
ENST00000642875.1:n.1082-209_1082-208del
ENST00000644120.1:n.1908-209_1908-208del
ENST00000644650.1:c.614-209_614-208del
ENST00000644905.1:n.1607-209_1607-208del
ENST00000644969.2:c.1638-209_1638-208del MANE Plus Clinical	ENSP00000496776.1:n.1638-209_1638-208del
ENST00000646730.1:c.1518-209_1518-208del	ENSP00000494784.1:n.1518-209_1518-208del
ENST00000646891.1:c.1518-209_1518-208del	ENSP00000493543.1:n.1518-209_1518-208del
ENST00000647434.1:c.561-209_561-208del	ENSP00000495132.1:n.561-209_561-208del
ENST00000288602.10:c.1518-209_1518-208del	ENSP00000288602.6:n.1518-209_1518-208del
ENST00000496384.6:c.341-209_341-208del
ENST00000497784.1:c.1553-209_1553-208del	ENSP00000420119.1:n.1553-209_1553-208del
NM_004333.4:c.1518-209_1518-208del , LRG_299t1:c.1518-209_1518-208del	NP_004324.2:n.1518-209_1518-208del
XM_005250045.1:c.1518-209_1518-208del	XP_005250102.1:n.1518-209_1518-208del
XM_005250046.1:c.1518-209_1518-208del	XP_005250103.1:n.1518-209_1518-208del
XM_011516529.1:c.1518-209_1518-208del	XP_011514831.1:n.1518-209_1518-208del
XM_011516530.1:c.1518-209_1518-208del	XP_011514832.1:n.1518-209_1518-208del
XR_242190.1:n.1526-209_1526-208del
XR_927520.1:n.1526-209_1526-208del
XR_927521.1:n.1526-209_1526-208del
XR_927522.1:n.1526-209_1526-208del
XR_927523.1:n.1526-209_1526-208del
NM_001354609.1:c.1518-209_1518-208del	NP_001341538.1:n.1518-209_1518-208del
NM_004333.5:c.1518-209_1518-208del	NP_004324.2:n.1518-209_1518-208del
NR_148928.1:n.1823-209_1823-208del
XM_017012558.1:c.1638-209_1638-208del	XP_016868047.1:n.1638-209_1638-208del
XM_017012559.1:c.1638-209_1638-208del	XP_016868048.1:n.1638-209_1638-208del
XR_001744857.1:n.1646-209_1646-208del
XR_001744858.1:n.1646-209_1646-208del
NM_001354609.2:c.1518-209_1518-208del	NP_001341538.1:n.1518-209_1518-208del
NM_001374244.1:c.1638-209_1638-208del	NP_001361173.1:n.1638-209_1638-208del
NM_001374258.1:c.1638-209_1638-208del MANE Plus Clinical	NP_001361187.1:n.1638-209_1638-208del
NM_004333.6:c.1518-209_1518-208del MANE Select	NP_004324.2:n.1518-209_1518-208del
NM_001378467.1:c.1527-209_1527-208del	NP_001365396.1:n.1527-209_1527-208del
NM_001378468.1:c.1518-209_1518-208del	NP_001365397.1:n.1518-209_1518-208del
NM_001378469.1:c.1452-209_1452-208del	NP_001365398.1:n.1452-209_1452-208del
NM_001378470.1:c.1416-209_1416-208del	NP_001365399.1:n.1416-209_1416-208del
NM_001378471.1:c.1407-209_1407-208del	NP_001365400.1:n.1407-209_1407-208del
NM_001378472.1:c.1362-209_1362-208del	NP_001365401.1:n.1362-209_1362-208del
NM_001378473.1:c.1362-209_1362-208del	NP_001365402.1:n.1362-209_1362-208del
NM_001378474.1:c.1518-209_1518-208del	NP_001365403.1:n.1518-209_1518-208del
NM_001378475.1:c.1254-209_1254-208del	NP_001365404.1:n.1254-209_1254-208del